Publication | Closed Access
Synthesis and Preliminary Biological Studies of 3-Substituted Indoles Accessed by a Palladium-Catalyzed Enantioselective Alkene Difunctionalization Reaction
233
Citations
9
References
2010
Year
Combinatorial ChemistryBioorganic ChemistryEngineering3-Substituted IndolesMolecular ComplexityPreliminary Biological StudiesOrganic ChemistryRelevant Indole FrameworkChemistryMedicinal ChemistryBiochemistryCatalysisPharmacologyNatural Product SynthesisAsymmetric CatalysisEnantioselective SynthesisBiomolecular EngineeringNatural SciencesMcf-7 CellsSynthetic ChemistryDrug Discovery
A unique alkene difunctionalization reaction that allows rapid construction of molecular complexity around the biologically relevant indole framework has been developed. The reaction proceeds with up to 87% yield, 99:1 er, and >20:1 dr. Evaluation of several of the compounds revealed promising anticancer activity against MCF-7 cells.
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